DePuy Mitek Straightshot Ligament Graft Passer/Protector, 11.5 mm Catalog Number : 232220
FDA Recall Z-0161-06 · Posted 2005-11-18
Recalling FirmDepuy Mitek, a Johnson & Johnson Co.
Recall StatusTerminated
Product CodeLXH
Date Initiated2005-08-09
Date Terminated2006-05-02
Product Quantity5 boxes /10 units (50 pieces)
Reason for Recall
Mislabeled: The kit contained the incorrect Ligament Passer. The package contained a 9.5 mm instead of the labeled 11.5mm ligament passer
Firm Action
DePuy Mitek notified the accounts by US Mail on 8/09/05. Accounts were requested to return product.
Root Cause
Other
Distribution Pattern
CA, NC, VA
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.